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G.P.1.03 King-Denborough syndrome associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene

✍ Scribed by J. Dowling; S. Lillis; K. Amburgey; S. Leber; H. Zhou; S. Al-Sarraj; E. Wraige; S. Abbs; C. Sewry; F. Muntoni; H. Jungbluth

No coin nor oath required. For personal study only.

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